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2017 Journal Article A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editingBell, Scott, Peng, Huashan, Crapper, Liam, Kolobova, Ilaria, Maussion, Gilles, Vasuta, Cristina, Yerko, Volodymyr, Pan Wong, Tak and Ernst, Carl (2017). A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing. Stem Cells Translational Medicine, 6 (3), 886-896. doi: 10.1002/sctm.16-0158 |
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2017 Journal Article Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTRRowe, Steven M., McColley, Susanna A., Rietschel, Ernst, Li, Xiaolei, Bell, Scott C., Konstan, Michael W., Marigowda, Gautham, Waltz, David and Boyle, Michael P. (2017). Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR. Annals of the American Thoracic Society, 14 (2), 213-219. doi: 10.1513/AnnalsATS.201609-689OC |
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2017 Journal Article Implication of LRRC4C and DPP6 in neurodevelopmental disordersMaussion, Gilles, Cruceanu, Cristiana, Rosenfeld, Jill A., Bell, Scott C., Jollant, Fabrice, Szatkiewicz, Jin, Collins, Ryan L., Hanscom, Carrie, Kolobova, Ilaria, de Champfleur, Nicolas Menjot, Blumenthal, Ian, Chiang, Colby, Ota, Vanessa, Hultman, Christina, O'Dushlaine, Colm, McCarroll, Steve, Alda, Martin, Jacquemont, Sebastien, Ordulu, Zehra, Marshall, Christian R., Carter, Melissa T., Shaffer, Lisa G., Sklar, Pamela, Girirajan, Santhosh, Morton, Cynthia C., Gusella, James F., Turecki, Gustavo, Stavropoulos, Dimitri J., Sullivan, Patrick F. ... Ernst, Carl (2017). Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics, Part A, 173 (2), 395-406. doi: 10.1002/ajmg.a.38021 |
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2017 Journal Article Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complicationPiccolo, Francesco, Tai, Anna Sze, Ee, Hooi, Mulrennan, Siobhain, Bell, Scott and Ryan, Gerard (2017). Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication. Respirology Case Reports, 5 (1) e00204, e00204. doi: 10.1002/rcr2.204 |
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2017 Journal Article Limitations to providing adult cystic fibrosis care in Europe: results of a care centre surveyMadge, Susan, Bell, Scott C., Burgel, Pierre- Régis, De Rijcke, Karleen, Blasi, Francesco and Elborn, J. Stuart (2017). Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey. Journal of Cystic Fibrosis, 16 (1), 85-88. doi: 10.1016/j.jcf.2016.07.001 |
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2017 Journal Article Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled TrialMontgomery, Shaylyn H., Shamji, Colleen M., Yi, Grace S., Yarnold, Cynthia H., Head, Stephen J., Bell, Scott C. and Schwarz, Stephan K. W. (2017). Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial. Regional Anesthesia and Pain Medicine, 42 (1), 25-31. doi: 10.1097/AAP.0000000000000522 |
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2017 Journal Article JCF - 2016Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). JCF - 2016. Journal of Cystic Fibrosis, 16 (1), 6-6. doi: 10.1016/j.jcf.2016.12.014 |
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2016 Journal Article Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacteriumBryant, Josephine M., Grogono, Dorothy M., Rodriguez-Rincon, Daniela, Everall, Isobel, Brown, Karen P., Moreno, Pablo, Verma, Deepshikha, Hill, Emily, Drijkoningen, Judith, Gilligan, Peter, Esther, Charles R., Noone, Peadar G., Giddings, Olivia, Bell, Scott C., Thomson, Rachel, Wainwright, Claire E., Coulter, Chris, Pandey, Sushil, Wood, Michelle E., Stockwell, Rebecca E., Ramsay, Kay A., Sherrard, Laura J., Kidd, Timothy J., Jabbour, Nassib, Johnson, Graham R., Knibbs, Luke D., Morawska, Lidia, Sly, Peter D., Jones, Andrew ... Floto, R. Andres (2016). Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium. Science, 354 (6313), 751-757. doi: 10.1126/science.aaf8156 |
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2016 Journal Article Lesch-Nyhan syndrome: Models, theories, and therapiesBell, Scott, Kolobova, Ilaria, Crapper, Liam and Ernst, Carl (2016). Lesch-Nyhan syndrome: Models, theories, and therapies. Molecular Syndromology, 7 (6), 302-311. doi: 10.1159/000449296 |
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2016 Journal Article Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktykiSmyth, Alan R., Bell, Scott C., Bojcin, Snezana, Bryon, Mandy, Duff, Alistair, Flume, Patrick, Kashirskaya, Nataliya, Munck, Anne, Ratjen, Felix, Schwarzenberg, Sarah Jane, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Taccetti, Giovanni, Ullrich, Gerald and Wolfe, Sue (2016). Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki. Pediatria Polska, 91 (Supp.1), S30-S53. doi: 10.1016/j.pepo.2016.08.014 |
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2016 Journal Article The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysisRamsay, Kay A., Sandhu, Harpreet, Geake, James B., Ballard, Emma, O'Rourke, Peter, Wainwright, Claire E., Reid, David W., Kidd, Timothy J. and Bell, Scott C. (2016). The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis. Journal of Cystic Fibrosis, 16 (1), 70-77. doi: 10.1016/j.jcf.2016.07.010 |
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2016 Journal Article Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort studyWells, J. Michael, Farris, Roopan F., Gosdin, Taylor A., Dransfield, Mark T., Wood, Michelle E., Bell, Scott C. and Rowe, Steven M. (2016). Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study. Lancet Respiratory Medicine, 4 (8), 636-645. doi: 10.1016/S2213-2600(16)30105-9 |
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2016 Journal Article The role of anaerobic bacteria in the cystic fibrosis airwaySherrard, Laura J., Bell, Scott C. and Tunney, Michael M. (2016). The role of anaerobic bacteria in the cystic fibrosis airway. Current Opinion in Pulmonary Medicine, 22 (6), 637-643. doi: 10.1097/MCP.0000000000000299 |
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2016 Journal Article A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory diseaseJohnson, Graham R., Knibbs, Luke D., Kidd, Timothy J., Wainwright, Claire E., Wood, Michelle E., Ramsay, Kay A., Bell, Scott C. and Morawska, Lidia (2016). A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease. PLoS One, 11 (7) e0158763, e0158763. doi: 10.1371/journal.pone.0158763 |
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2016 Journal Article A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patientsFlume, Patrick A., VanDevanter, Donald R., Morgan, Elizabeth E., Dudley, Michael N., Loutit, Jeffery S., Bell, Scott C., Kerem, Eitan, Fischer, Rainald, Smyth, Alan R., Aaron, Shawn D., Conrad, Douglas, Geller, David E. and Elborn, J. Stuart (2016). A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients. Journal of Cystic Fibrosis, 15 (4), 495-502. doi: 10.1016/j.jcf.2015.12.004 |
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2016 Journal Article The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registryStephenson, Anne L. and Bell, Scott C. (2016). The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry. Annals of the American Thoracic Society, 13 (7), 1014-1015. doi: 10.1513/AnnalsATS.201604-250ED |
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2016 Journal Article Methicillin-resistant Staphylococcus aureus acquisition in healthcare workers with cystic fibrosis: a retrospective cross-sectional studyWood, Michelle E., Sherrard, Laura J., Ramsay, Kay A., Yerkovich, Stephanie T., Reid, David W., Kidd, Timothy J. and Bell, Scott C. (2016). Methicillin-resistant Staphylococcus aureus acquisition in healthcare workers with cystic fibrosis: a retrospective cross-sectional study. BMC Pulmonary Medicine, 16 (78) 78, 1-7. doi: 10.1186/s12890-016-0243-z |
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2016 Journal Article A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature reviewMerner, Nancy, Forgeot d'Arc, Baudouin, Bell, Scott C., Maussion, Gilles, Peng, Huashan, Gauthier, Julie, Crapper, Liam, Hamdan, Fadi F., Michaud, Jacques L., Mottron, Laurent, Rouleau, Guy A. and Ernst, Carl (2016). A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. American Journal of Medical Genetics Part A, 170 (5), 1225-1235. doi: 10.1002/ajmg.a.37566 |
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2016 Journal Article High ambient temperature and risk of intestinal obstruction in cystic fibrosisOoi, Chee Y., Jeyaruban, Christina, Lau, Jasmine, Katz, Tamarah, Matson, Angela, Bell, Scott C., Adams, Susan E. and Krishnan, Usha (2016). High ambient temperature and risk of intestinal obstruction in cystic fibrosis. Journal of Paediatrics and Child Health, 52 (4), 430-435. doi: 10.1111/jpc.13096 |
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2016 Journal Article Infection in cystic fibrosis: impact of the environment and climateRamsay, K. A., Stockwell, R. E., Bell, S. C. and Kidd, T. J. (2016). Infection in cystic fibrosis: impact of the environment and climate. Expert Review of Respiratory Medicine, 10 (5), 505-519. doi: 10.1586/17476348.2016.1162715 |
